BEUDAMED
    10 results · 23ms · Sources: EU EUDAMED, US FDA

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    LuminScan (TM) Imaging System

    FDA 510(k)
    FDA Class 2 ·Radiology

    Suprasorb

    FDA UDI
    Lohmann & Rauscher International GmbH & Co KG·04068225067105·

    ARTHREX INTERFERENCE SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FUJINON EPX-4440HD DIGITAL VIDEO PROCESSOR

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    GMK-PRIMARY TIBIAL TRAY FIXED CEMENTED SIZE 5 R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·January 8, 2020

    RATCHETING SCREWDRIVER HANDLE

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HXX·January 13, 2026

    IMPLANTED CATHETER

    FDA Adverse Event
    Malfunction ·C. R. BARD INC. (BASD)·Product code LJS·June 6, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 14, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC SINGAPORE OPERATIONS·Product code DTB·October 10, 2014

    OPTETRAK Three Peg Patella, Item Numbers: a) 200-02-26, 26MM; b) 200-02-29, 29MM; c) 200-02-32, 32MM; d) 200-02-35, 35MM; e) 200-02-38, 38MM; f) 200-02-41, 41MM;

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·June 26, 2024